doxycycline

Generic: doxycycline

Labeler: northwind health company, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxycycline
Generic Name doxycycline
Labeler northwind health company, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

doxycycline 100 mg/1

Manufacturer
Northwind Health Company, LLC

Identifiers & Regulatory

Product NDC 51655-350
Product ID 51655-350_49d7ff1e-293a-4374-e063-6394a90aad44
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091605
Listing Expiration 2027-12-31
Marketing Start 2022-11-29

Pharmacologic Class

Established (EPC)
tetracycline-class drug [epc]
Chemical Structure
tetracyclines [chemical/ingredient]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51655350
Hyphenated Format 51655-350

Supplemental Identifiers

RxCUI
1650142
UNII
N12000U13O
NUI
N0000175882 N0000007948

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name doxycycline (source: ndc)
Generic Name doxycycline (source: ndc)
Application Number ANDA091605 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 20 TABLET in 1 BOTTLE, PLASTIC (51655-350-20)
source: ndc

Packages (1)

51655-350-20 20 TABLET in 1 BOTTLE, PLASTIC (51655-350-20)

Ingredients (1)

doxycycline (100 mg/1)

Linked Drug Pages (1)

Doxycycline ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "49d7ff1e-293a-4374-e063-6394a90aad44", "openfda": {"nui": ["N0000175882", "N0000007948"], "unii": ["N12000U13O"], "rxcui": ["1650142"], "spl_set_id": ["f2f1ee15-9323-1263-e053-2995a90a01fa"], "pharm_class_cs": ["Tetracyclines [Chemical/Ingredient]"], "pharm_class_epc": ["Tetracycline-class Drug [EPC]"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (51655-350-20)", "package_ndc": "51655-350-20", "marketing_start_date": "20221129"}], "brand_name": "Doxycycline", "product_id": "51655-350_49d7ff1e-293a-4374-e063-6394a90aad44", "dosage_form": "TABLET", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "51655-350", "generic_name": "Doxycycline", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline", "active_ingredients": [{"name": "DOXYCYCLINE", "strength": "100 mg/1"}], "application_number": "ANDA091605", "marketing_category": "ANDA", "marketing_start_date": "20221129", "listing_expiration_date": "20271231"}